Hip Replacement Scheduled :: Feeling Nervous About The Amount Of Pain
Apr 3, 2016
Next Friday I am having my right hip replaced and I'm feeling really nervous , the main reason I'm feeling nervous is amount of pain I possibly could be in after the op and how much or little getting up and about when I get home . I'm 42 and really fit at the moment and exercise a few times a week , so I'm not looking forward to be house bound for a while . But I am looking forward to a few months down the road once everything starts healing (hopefully).
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I finally scheduled my total bilateral joint replacement for Jan. 15, 2014. As you can imagine I am very nervous. Just yesterday I had screws removed from my latest surgery on September 13th. Back on September 13th, I was to have undergone a bilateral arthrotomy with fat grafting but unfortunately I had some scary complications and that particular procedure was not done. I ended up having an exploration of the left neck, open reduction and internal fixation of the left mandible, extraoral vertical ramus osteotomy and condylectomy and an open left TMJ arthroplasty. Plus I had a left cranial base bleed which I was sent emergently from the OR to interventional radiology to locate and control and bleed and spent several days on a ventilator in the ICU.
Currently, my bite is so off to the left side that it is not even funny. I look like Rocky from the movie "Rocky" when he is screaming...."Adrianne!!" and his mouth is sort of way off to one side.
Can anyone out there who has had TMJ Concepts joints replaced lend me any guidance or advice? I am unable to chew and have been on a non chewing diet since March and am only able to open my mouth two fingers and talking hurts quite a bit.
I know I am making the right decision for me as I have been dealing with this for years.
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All set for my TKR tomorrow - it may sound strange to some people but after such a long wait for this - I am really looking forward to this operation !! I have to be at the hospital at 7am and have been told that I am first on the list as type 2 diabetic - I am not worried about the pain post op as can be much worse than the pain this knee has dished out so far. Wish me luck - they are keeping me in for 5 days so will communicate again next weekend, with some positive comments I hope.
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For the past half year I am feeling tingling feet. And now “electrical” pain is occurring. I am obese and my husband says it is because of that... could be...
Any other suggestions?
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Been on venlafaxine since 3 months. I'm up to 225 mg which seemed to working a treat, however, I do get the odd day of anxiety here and there. Today is probably the worst. It started as racing heart a few days ago. Now I'm getting the tinglings, nervous tummy, feeling a bit down. I'm really scared that I've got treatment resistance depression/anxiety.
I took some MDMA whilst on holiday last June, which kicked this whole thing off.
It's just so soul destroying as I felt on top of the world earlier this week.
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Is anyone past that time yet? Will this tight feeling in my hip eventually go away? I don't have pain however, I still can't walk a long way without the tight feeling bothering me.
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Day five almost on the books...I have done all my exercises and walked several times...even outside. my question for those of you with THR experience... when walking, did you feel a bit uneven? Is this normal? Is it from swelling?
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I'm exactly 1 week overdue and i'm scheduled for an induction in 6 hours! I really don't want to be induced. I feel the baby could come on its own very soon and i rather give him a few more days. I'm wondering has anyone been induced? the more i read about induction the more im turned off by it! im young and healthy and i think extending for a few more days won't affect the baby.
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Approximately 8 years ago, doctors discovered a 4.6cm aneurysm in my aorta during routine testing in preparation for an upcoming surgery. Fast forward 8yrs later my aneurysm has increased in size to 5.8cm so everyone in these forums know what that means...its surgery time! I've had echoes and CT Scans every 6 months as this appears to be the wait and watch approach when aneurysms are under 5cm.. My aneurysm was slow growing until the last 18 months. At least 3 CT scans were missed and the echoes didn't clearly show growth. Now, I am terrified out of my mind about having an "open repair". It has been brought to my attention that because of the location of my aneurysm, I am not a candidate for an "endovascular repair". Imagine my disappointment. My anxiety level is at an all time high and I am symptomatic. Chest heaviness and back pain coupled with migraine headaches. Apart of me realizes that these surgeries are done rather routinely now but that still doesn't stop the horrendous fear I have. I have had severe allergic reactions to meds in the past. I'm not a good sleeper generally and now its worst. I have to schedule my surgery by June, to have at least 6 months of recovery time before my family cruise in Dec.. I am a 56yr old female veteran. I used to run least east 3 miles a day and Jazzercise at least 5 days a week until I was told to stop by my cardiologist. I have since gained about 15 lbs in these last 8yrs but other than that, no high cholesterol, high blood pressure or diabetes. My doctors assure me that I am a perfect candidate and shouldn't experience any complications but the idea of my sternum being cut open and just the entire procedure is frightening. What's more concerning is once you have aneurysm in one place, another could eventually show up somewhere else in the future. I've also been told that these repairs can require maintenance in the future! Its all just a little too much but knowing the alternative..carrying around a ticking time bomb, I have to have the surgery. I know people that survived a couple yrs after the surgery, had to have some type of maintenance and never truly recovered and died. My niece fiancé was life alighted to the hospital in mid March with a dissection, he is currently and the road to recovery. I have a lot of family support but of course they are all concerned as well. The saga continues..
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Well my date for my hysterectomy is in two days ( Wednesday) I'm absolutely petrified, I'm not sleeping and I feel so nervous.
Any advice from any of you lovely ladies would be so much appreciated right now. Because at this point in time I feel like running in the opposite direction.
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I am having a da vinci robotic laparoscopic myomectomy on Tuesday and I am really scared. I am scared of the general anesthesia, I am scared of the pain meds and recovery. I am scared of not being able to do things. I am even scared of being scared. Anybody else go through this surgery that could ease my mind...only positive stories please I can't take anything negative.
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So, I have my date! June! Excited and nervous all at the same time, I'm reading lots lately about swelling, pain and being off your feet longer than you thought. This IS a difficult surgery, and I know it's not going to be easy. Trying to put some positive vibes out, and remembering why you did this, is anyone brave enough to show off their tootsies? Maybe before and after? A lot to ask I know.
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I am going in tomorrow to have my cyst and fibroid removed.could anyone tell me what happens once you get there.i have to go for 11 am an have been told I should go down by 2pm.
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It started one Saturday night when after a long day of doing overtime at work, followed by handing in my degree dissertation, I could not eat very much going to bed and was waking up a lot during the night because I was hungry, but when I tried to eat I couldn't stomach much. I went to the doctors on the Tuesday and she suggested it was just a bug as I was so tired and had very little energy. She took bloods which all came back fine. I felt a little better a week later but still not right but tried to put it at the back of my mind. However, every so often I would have an episode where I was feeling sick and had stomach pains and I could not each much so I lost a lot of weight.
The doctor prescribed me with domperidone in September which helped for a number of months but stomach was still not right.
Fast forward to 4 weeks ago I wasn't feeling too bad and was managing to get on with day to day life with some limitations (because of my stomach issues, I cannot drink alcohol, coffee or fizzy drinks) so I rarely go out. The doctor diagnosed me with stress and anxiety and I have recently started speaking to a therapist through work.
But basically, for the last four weeks I have been feeling sick all day every day with stomach pains a few times a day which prevents me from getting on with day to day life. It started the day after I had sex and the day after that I had my period as well as a cold. These pains do not seem to be getting any better and seems to help when I have something to eat, but I cannot face eating a lot. For example, bananas help but I don't want to have too many a day as they have bloated me in the past.
A couple of nights ago I woke up with a tremendous pain down the left side of my stomach which then moved over into the centre. I still feel sick but feel much better when I am out and about walking for example, but its just a lot of effort to get up and about when sometimes i do not want to get out of bed.
This condition is stopping me from leading a normal active, well life. I am only 24 and cannot seem to lead a normal life in comparison to my friends who can. The docs still say this is down to stress and anxiety but it has to be much more than that. I get the impression that my parents, friends and work colleagues do not understand and the fact that the pain is constant does nothing to lower my stress and anxiety levels as I always have to make sure I take food with me wherever I go and can't go too long without food.
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i took primolut medicine from 25th april to 30th april 2 pills daily . today is 5th of may not came period yet.. i have to go for umrah on 13th of this month . before that i have to get it done my periods. last 3 month onwards i dont have period ..
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It's 3 weeks today since I've done my myomectomy. I'm still a little swollen and I get either sharp shooting pains or what feels like cramps in the area. I think maybe it's my bladder that's cramping ? because I feel a slight discomfort when I pee. I still get tired very easily, even if all I'm doing is walking around the house. I lost 1.3 litres of blood and my blood count's lot less than what it should be. Is that the reason why ? I was supposed to do a blood count on Monday 23rd but I didnt go because I wanted the boyfriend to come with me to bolster me. My biggest fibroid was almost the size of a football and the second biggest was the size of a grapefruit. I got lots of rest last week but I still feel tired..I don't understand why. I'm feeling just as awful as I did after the surgery. I thought the tiredness and pain would be gone by now. I have to go back to work tomorrow but my doctor said 6 weeks. I don't want to lose my job. My boyfriend says I'm fine. It's week 3 now. Also,my left lymph gland/groin hurts sometimes. I'm back to feeling the same discomfort as I did after the myomectomy. The scar area is a mixture of numbness and pain. Is this normal ? My sides and back hurt too. I've been using my abdominl muscles to get up, which I didn't do before, (I was using my hands to push up and my boyfriend would help me to get up), so now my abs feel sore. Is that okay ? My doctor had said that if my blood count doesnt go back up to normal I may have to do a blood transfusion. I don't want to do that. I've stopped taking the pain medication Voltaren, because I don't want to get addicted.
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I'm only 17 years old. I have felt the way i feel now for months. I am not pregnant before anyone suggests that!
I suffered from a disease/illness where my glands swelled up til they were huge and you could clearly see them. I had a fever all day, i would go cold and the hot, i had no energy at all and was generally sick! The doctor gave me some antibiotics and it cleared up.
Ever since then i have not been myself. I feel sick at some point during the day, i constantly have a weird feeling in my head, its not pain as such, but like a numbing feeling and irritation. I feel like im going to faint all the time, im weak and very tired, i also get chest pains from time to time & my breathing is rubbish, its hard to breath at times, i generally feel like im dying
I have had countless blood tests and all of them showed nothing!
This totally upset me because im frustrated, i just want it to be over!!
The doctor told me just to have lots of water and exercise.
My family were convinced that i suffer from anxiety and panic attacks!
As i had a panic attack due to the fact i felt so ill i thought i was dying!
It wasn't just happening to me for no reason the attack.
so they took me to the doctor where he told me my symptoms were that of anxiety and panic attacks so he gave me some tablets to take.
But i still feel the same!!
I do not believe that i have anxiety
I am sick if people believing that is what it is!!
.......
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I am slightly worried, but last thursday i was told i had asthma and i was given 2 inhalers, but since then my breathing has gotten worse, i suffer from chest pain and a "that's not right" feeling in my chest, and i am soooo fatigued and have no energy and now have lost my appetite :-(
and also feel sometimes light headed, I have been given a blood test but results aren't out yet and i hate waiting also i am really worried which make me worse and i have some back pain as well.
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Can someone give insight? Been to doc, told hemorrhoids. Along with anal tear. Should I move on to a second opinion?
Still lots of pain, no blood any more. Throbbing , fullness feeling. She diagnosed me Monday and gave me some foam that has done nothing.
Been on miralax as well, no improvement.
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About 4 months ago I started noticing my both of my feet felt very fatigued after a short walk and when I put my feet up to rest, the lower back side of my heels (below my achilles just before it turns to the underside of my foot) felt slightly irritated. The fatigue in my feet would come and go then about 6 weeks ago I started feeling pain/discomfort in the bottom of my feet (in the heel area). The pain has never been worse in the morning. It gets worse the more I'm on my feet (especially standing or slow walking like when shopping). I have extremely high arches and the doctor thinks I am experiencing pain because of the anatomy of my feet (a lot of concentrated force on the heels).
Let me rewind a bit. Because of my very high arches I have been fearful of developing foot problems, especially PF. As a result, in March of this year I started doing calf stretches in the morning. About 30 minutes to an hour after waking up I would stand on a stair and really stretch out my calves (3 sets of 20 seconds for both legs). It was about 6-7 weeks later that at the same time I started noticing the pain in both of my heels.
About 3 weeks ago I got custom orthotics and shoes with excellent cushioning for the heels. About 10 days ago I stopped stretching thinking I may have actually injured myself because of overstretching.
I have no pain when pressing on my heels or achilles or anywhere under my feet, just an inflamed irritated feeling when I walk. Other than a few steps here and there I don't walk barefoot and haven't for the past couple of years (broke and ankle two years ago and hard surfaces really aggravated things after getting out of the cast).
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I have my second hp (right) done 2 weeks ago. I had a terrible sciatica pain till the op. Now there is a less sciatica pain though, I still feel the nerve is irritated since I still feel the stretch on my hamstring. I was wishing that it was going to go away after thr, but it seems it will come back after I bear normal weight on my leg.
Is there anybody who got rid of sciatica pain and how did you do that ?
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